Cosmetic recalls
21 federal recalls in the last 12 months. Federal recalls for cosmetic products. Sourced from the FDA.
- 2026-04-22FDA-DrugIsland Kinetics, Inc. d.b.a. CoValence LaboratoriesClass IIStop using Skin Script Blemish Spot Treatment
Island Kinetics, Inc. (d.b.a. CoValence Laboratories) is recalling specific lots of Skin Script Blemish Spot Treatment because the product failed stability testing. This means the product may not maintain its intended strength or safety over time. No injuries have been reported.
- 2026-04-22FDA-DrugOwen Biosciences Inc.Class IIStop using HydroPeptide Clear Alliance Serum
HydroPeptide Clear Alliance Serum (2.5% benzoyl peroxide) contains benzene, a harmful chemical not intended in the product. The affected bottles are 1 FL OZ and 2 FL OZ sizes with lot numbers 2518800 and 2518900. No injuries have been reported, but the FDA has issued a recall due to potential health risks from benzene exposure.
- 2026-04-22FDA-DrugOwen Biosciences Inc.Class IIStop using FarmHouse Fresh acne lotion
FarmHouse Fresh Midnight Clearing night lotion (2.5% benzoyl peroxide) contains benzene, a harmful chemical not meant to be in this product. The contamination was found in three specific lot numbers. No injuries have been reported so far.
- 2026-04-09FDA-PRStop using Morovan nail polish remover
Morovan gel nail polish remover (15ml bottle, turquoise with white cap) was found to contain methylene chloride and chloroform—chemicals prohibited in cosmetics. Methylene chloride may cause cancer and is not allowed in cosmetics at any level under FDA regulations. About 4,000 units were sold on Amazon between August 2025 and January 2026.
- 2026-01-21FDA-DrugGOLD STAR DISTRIBUTION INCClass IIStop using recalled Colgate and Crest toothpaste
Several Colgate and Crest toothpaste products distributed by Gold Star Distribution Inc. were stored in conditions with rodent exposure and activity. The FDA found insanitary conditions at the distribution center that do not meet manufacturing standards. No injuries have been reported.
- 2026-01-21FDA-DrugGOLD STAR DISTRIBUTION INCClass IICheck your Axe and Lucky deodorants
Gold Star Distribution Inc. distributed multiple Axe body sprays and Lucky deodorant products that were stored in conditions with rodent activity. The FDA found insanitary handling at their distribution center. No injuries have been reported.
- 2026-01-21FDA-DrugGOLD STAR DISTRIBUTION INCClass IIStop using recalled petroleum jelly products
Gold Star Distribution Inc. distributed several petroleum jelly products that were stored in insanitary conditions, including exposure to rodents, at their distribution center. The affected products include Vaseline, Lucky, Personal Care, and Softee petroleum jelly in various sizes and formulations. All lots distributed by Gold Star that have not expired may be affected.
- 2026-01-21FDA-DrugGOLD STAR DISTRIBUTION INCClass IIStop using Lucky Ice Cool Mouthwash
Lucky Ice Cool Mouthwash was distributed from a facility with insanitary conditions, including rodent exposure and activity. The FDA is recalling all unexpired lots of this product due to potential contamination from the distribution center conditions.
- 2026-01-21FDA-DrugGOLD STAR DISTRIBUTION INCClass IIStop using Gold Star vaporizing chest rub
Gold Star Distribution's 4 oz vaporizing chest rub was distributed from a facility with insanitary conditions, including rodent exposure. The product may have been contaminated during storage or handling at their distribution center.
- 2026-01-21FDA-DrugGOLD STAR DISTRIBUTION INCClass IIStop using Gold Star Distribution ice gel
Gold Star Distribution's 8oz ice gel products were stored in conditions where rodents were present in their distribution center. The FDA found insanitary conditions that do not meet required manufacturing and distribution standards. All unexpired lots distributed by this company are affected.
- 2026-01-14FDA-DrugSignature Formulations, LLCClass IIStop using ORL Kids Natural Toothpaste
ORL Labs recalled ORL Kids Natural Toothpaste in Bubblegum Flavor due to deviations from manufacturing quality standards (cGMP). The affected product is Lot #250520P4 with expiration date 05/27, distributed in Arizona. No injuries have been reported.
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IICLEARSTEM YOU ARE SUNSHINE SPF 50, Zinc Oxide 21%, 2.1 oz/61g per bottle, Distributed by: CLEARSTEM Skincare, clearstemskincare.com. NDC: 35192-046-17
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIElixir by Coco March Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-050-17, UPC 6 7229 99913 8
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIElixir by Coco March Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz (62g) per bottle, Distributed by: VitaTienda Co U.S.A., San Juan, PR 00646. NDC: 35192-048-17, UPC 8 10145 82007 0
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IISugared+Bronzed Tinted Mineral Sunscreen SPF 50, Zinc Oxide 21%, Net WT 3.3 OZ (93 G) per tube, Dist. By: Sugared+Bronzed, 929 Montana Ave, Santa Monica, CA 90403. NDC: 35192-055-18, UPC 8 50047 92223 6
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIKarina Daily Moisturizer SPF 25, Octinoxate 7.5% and Zinc Oxide 7.0%, Net WT. 5 oz/ 141.7 g per tube, Dist. By: Beauty4Pros LLC, Palm Desert, CA 92211. NDC: 35192-033-16, UPC 8 18204 02572 5
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIGabriel Mineral Sunscreen SPF 50, Zinc Oxide 21%, 2.1 oz, Net 61 g per tube, Dist. By: Gabriel Cosmetics, Inc., Redmond, WA USA 98052, NDC: 35192-044-01, UPC 7 07060 9592 1
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIDoctor D. Schwab Shimmery Sun Lotion Sunscreen SPF 30, Titanium Dioxide 5% and Octinoxate 4%, 4 oz./113.4 g per tube, Doctor D. Schwab, A division of CA BOTANA, San Diego, CA 92121. NDC: 35192-012-02
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IISea Enzyme Ultra Umbrella Sunscreen SPF 30, Titanium Dioxide 4%, Octinoxate 4%, 4 oz./113.4 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-011-02
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIDoctor D. Schwab Flawless Skin Fluid Tinted Moisturizer SPF 50, Zinc Oxide 21%, 2.1 oz/61 g per tube, Manufactured by CA BOTANA, San Diego, CA 92121. NDC: 35192-043-17
CGMP Deviations
- 2025-12-03FDA-DrugCA BOTANA International, Inc.Class IIDoctor. D. Schwab Mineral Sunscreen SPF 50, Zinc Oxide 21%, 4 oz./ 113.4 g per tube, Manufactured by CA Botana, San Diego, CA 92123. NDC: 35192-042-02
CGMP Deviations
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